Canonical Allele Identifier: PA915978922
Gene: ASB10 HGNC NCBI

Linked Data

ClinVar Variation Id: 99958
ClinVar RCV Id: RCV000086408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135932.2:p.Asn175Thr
CA150494
NM_001142460.1:c.524A>C